Taiwan FDA registration 8364e768d322a1bf5b92c395bf7d82da
“Medtronic” IN.PACT Pacific Paclitaxel-eluting PTA Balloon Catheter
TW: “美敦力”派斯飛克紫杉醇塗藥周邊球囊導管
Registration details
- Analysis ID
- 8364e768d322a1bf5b92c395bf7d82da
- License Form
- Ministry of Health Medical Device Import No. 028910
- Customs Code
- DHA05602891005
Company information
- Manufacturer
- MEDTRONIC IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 15, 2016
- Expiry Date
- Nov 15, 2026
About this record
Access comprehensive regulatory information for “Medtronic” IN.PACT Pacific Paclitaxel-eluting PTA Balloon Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8364e768d322a1bf5b92c395bf7d82da and manufactured by MEDTRONIC IRELAND. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices